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January 24, 2024WanaBana Fruit Pouches Causing Lead Poisoning Lawsuit
January 24, 2024
What is Zantac?
Zantac (generic name: ranitidine) was a heartburn medication used to reduce stomach acid, treating conditions like acid reflux, heartburn, and ulcers. It was widely available both over-the-counter (OTC) and by prescription for decades, until it was pulled from the market in 2020 due to safety concerns regarding cancer caused by the breakdown of ranitidine into NDMA. Reports indicate that the levels of NDMA in Zantac can be up to 26,000 times higher than the FDA’s acceptable limit – posing a significant cancer risk in users.
How Does Zantac Potentially Cause Cancer?
This issue with Zantac is linked to dangerously high levels of N-nitrosodimethylamine (NDMA), a chemical classified as a probable human carcinogen (cancer-causing substance) by the World Health Organization (WHO) and the Environmental Protection Agency (EPA).
Why is There NDMA in Ranitidine?
As an unstable chemical, studies found that ranitidine can degrade into NDMA over time, especially when exposed to heat and humidity (such as during storage and transportation).
Unlike contamination issues in other drugs, the problem with Zantac is not external contamination — it’s that ranitidine itself can break down into NDMA.
How is NDMA Linked to Cancer?
NDMA has been shown to cause cancer in lab animals.
High exposure to NDMA in humans has been associated with increased risks of bladder, stomach, liver, esophageal, pancreatic, and colorectal cancer.
Potential NDMA Exposure from Long-Term Use of Zantac
Some lawsuits claim that regular Zantac use led to dangerous levels of NDMA exposure, far exceeding the FDA’s daily intake limit of 96 nanograms of NDMA.
Some independent tests suggested that a single 300 mg Zantac pill could generate over 3,000,000 nanograms of NDMA.
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Why Was Zantac Removed from the Market?
In April 2020, the FDA requested all ranitidine products, including Zantac, be withdrawn after testing confirmed that NDMA levels could increase over time, especially when stored at higher temperatures.
Zantac Lawsuits
The lawsuits allege that drug manufacturers knew or should have known about the risks of NDMA and failed to warn consumers.
Claims in the lawsuits:
Zantac caused cancers such as:
- Bladder Cancer
- Stomach Cancer
- Liver Cancer
- Pancreatic Cancer
- Esophageal cancer.
Manufacturers (Sanofi, GlaxoSmithKline, Pfizer, Boehringer Ingelheim) failed to warn consumers.
Plaintiffs seek compensation for medical expenses, lost wages, pain and suffering.
Eligibility for Zantac Cancer Lawsuits:
Individuals who took Zantac and developed cancer may be eligible to file a lawsuit. If you or a loved one used Zantac and have concerns about your health, our legal team is prepared to advocate for your rights and pursue the compensation you may be entitled to.
Dealing with the fallout from exposure to harmful substances can be daunting. Selinger Law is here to ensure you receive the support and guidance you need. Contact us today for a free case evaluation and to learn more about your legal options. Learn more about other dangerous medication here.